498-40-8
498-40-8
Chemical Structure
L-Cysteic acid
- CAS No.: 498-40-8
- Formula:C3H7NO5S
- Molecular Weight:169.16
IUPAC Name: sulfo-D-alanine
InChIKey: XVOYSCVBGLVSOL-REOHCLBHSA-N
SMILES: N[C@H](C(O)=O)CS(=O)(O)=O
Biological Activity: L-Cysteic acid is a non-proteinogenic amino acid. L-Cysteic acid modification enhances the inhibitory effects on ROS and MDA. The combination of L-Cysteic acid with Demecolcine (HY-N0282) maximizes CSADCase immunoreactivity. L-Cysteic acid modification enhances the antioxidant activity of collagen peptide CP. L-Cysteic acid can be used in studies of oxidative stress-induced damage[1][2][3][4].
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L-Cysteic acid | 98.0% | L-Cysteic acid is a non-proteinogenic amino acid. L-Cysteic acid modification enhances the inhibitory effects on ROS and MDA. The combination of L-Cysteic acid with Demecolcine (HY-N0282) maximizes CSADCase immunoreactivity. L-Cysteic acid modification enhances the antioxidant activity of collagen peptide CP. L-Cysteic acid can be used in studies of oxidative stress-induced damage. | ||||||||||||||||||||
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L-Cysteic acid (Standard) | 99.92% | L-Cysteic acid (Standard) is the analytical standard of L-Cysteic acid (HY-124009). This product is intended for research and analytical applications. L-Cysteic acid is a non-proteinogenic amino acid. L-Cysteic acid modification enhances the inhibitory effects on ROS and MDA. The combination of L-Cysteic acid with Demecolcine (HY-N0282) maximizes CSADCase immunoreactivity. L-Cysteic acid modification enhances the antioxidant activity of collagen peptide CP. L-Cysteic acid can be used in studies of oxidative stress-induced damage. | ||||||||||||||||||||
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References
- [1]. Jin H, et al. Regulation of HO-induced cells injury through Nrf2 signaling pathway: An introduction of a novel cysteic acid-modified peptide. Bioorganic chemistry. 2021 May;110:104811.
- [2]. Hernández-Ibáñez N, et al. Reprint of: l-Cysteine determination in embryo cell culture media using Co (II)-phthalocyanine modified disposable screen-printed electrodes[J]. Journal of Electroanalytical Chemistry, 2017, 793: 77-84.
- [3]. Wilson DF, et al. Transport of cysteate by synaptosomes isolated from rat brain: evidence that it utilizes the same transporter as aspartate, glutamate, and cysteine sulfinate. Journal of neurochemistry. 1986 Oct;47(4):1091-7. [Content Brief]
- [4]. Chan-Palay V, et al. Sagittal cerebellar microbands of taurine neurons: immunocytochemical demonstration by using antibodies against the taurine-synthesizing enzyme cysteine sulfinic acid decarboxylase. Proceedings of the National Academy of Sciences of the United States of America. 1982 Jul;79(13):4221-5.
